A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952882



Internal ID16955069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:91233057..91234056hg38UCSC Ensembl
Outerchr14:91699401..91700400hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998388
SamplesBILGI_BIOE
Known GenesGPR68
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952882
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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